Photorhodopsin
is a light sensitive pigment, similar to that found in the human eye. Until
recently, photorhodosin was only thought to be found in archaea, but using
molecular analysis Beja et al (2001) indicates that a different and diverse
form of photorhodopsin is widespread among bacteria. It has been shown that the
pigment is indeed light sensitive and acts as a proton pump, but does not
produce enough energy to fix carbon. The function of this pigment was therefore
less well-understood, and subject to debate among scientists.
In 2010,
Gomez-Consarnau and colleagues discovered that photorhodopsin functioned as a
solar powered booster pack, promoting survival when nutrient limitation
threatened. The bacterium they isolated was a Vibrio sp. (87% similarity with V.
harveyi), the first Vibrio. sp to be identified with the photorhodopsin gene
(PR). Interestingly, phylogenetic analysis clustered the PR gene with
Alphaproteobacteria, showing that the PR gene was acquired through horizontal
gene transfer.
To draw their
conclusion, they used experimental methodologies backed up using a
genetic-mutation. Firstly, a starvation experiments incubated bacteria in
different light treatments: continuous light; light/dark cycles - high light
(representing surface waters), low light (representing deeper water); no light,
without nutrients. Bacteria starved in continuous or high light had grown
40-60% more in size and was twice as abundant than bacteria without light,
suggesting that photorhodopsin was improving survival during starvation.
Furthermore, deletion of the PR gene (PR mutant) supported the role of
photorhodopsin as a light-harvesting pigment, as PR mutants did not show any
variation in survival fitness between the light treatments. Additionally
photorhodopsin helped the bacteria recover from starvation, as bacteria
supplied with nutrients after starvation had a 3-5 fold higher density in the
light compared to those in the dark, and PR mutants remained unresponsive to
different light treatments. This shows that energy provided by the
photorhodopsin helped bacteria respond to improved conditions, further
promoting their survival.
The abundance
and diversity of the PR gene is not surprising given its function. Nor that
this gene is passed horizontally, as it will provide a huge advantage in
nutrient poor open water. However, I question the necessity of this gene in the
Vibrio and think it may just reflect Vibrio’s opportunistic nature.
Copiotrophs cope with nutrient extremes by reducing and expanding their size,
further, they express rapid chemotaxis in order to source nutrients, which
gives them enhanced advantages in locating food anyway. However, Vibrio
are hugely successful and dominate due to this opportunistic nature, plus if
this gene was ‘available’ I can’t say I wouldn’t have done the same.
Reference:
Gómez-Consarnau, L.,
Akram, N., Lindell, K., Pedersen, A., Neutze, R., Milton, D. L., ...
& Pinhassi, J. (2010). Proteorhodopsin phototrophy promotes survival
of marine bacteria during starvation. PLoS biology, 8(4), e1000358.
Hi Kat - thanks for the post!
ReplyDeleteI think the photorhodopsin story is particularly interesting from an evolutionary perspective; how did it come to be - is it derived from a virus perhaps? I wondered if you knew of any studies which have examined this?
Thanks,
Jack
Very interesting point - I'm not sure of the origin - It makes sense that it evolved in the SAR11 - nutrient limited bacteria - the ones that perhaps needs a bit of a boost when nutrients is low - but this is just speculation. What is really interesting is the 'eco' types that are found within the rhodopsin, slight genetic variations of the pigment that allows them to utilise different wavelengths - similar to the prochloroccocus story.
ReplyDeleteThey didn't mention viruses - but viral lyogeny could indeed contribute to the spreading of this gene - esp as archaea have also need identified with it - not just the membrane form but this same energy booster pack! I'm not sure how easy archaea can use other modes of HGT..